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Promotion of neurovascular remodeling through mitochondria transfer after stroke

中风后通过线粒体转移促进神经血管重塑

基本信息

批准号：
9272019
负责人：
Kazuhide Hayakawa
金额：
$ 37.8万
依托单位：
MASSACHUSETTS GENERAL HOSPITAL
依托单位国家：
美国
项目类别：
财政年份：
2015
资助国家：
美国
起止时间：
2015-09-01 至 2020-05-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/9272019
关键词：
Astrocytes Blood Vessels Brain Brain Injuries Calcium Cells Central Nervous System Diseases Cicatrix Coculture Techniques Confocal Microscopy Culture Media Cyclic ADP-Ribose Data Electron Microscopy Endothelial Cells Endothelium Etiology Glucose HMGB1 gene Heat shock proteins Human In Vitro Inflammation Ischemia Knowledge Label Magnetic Resonance Imaging Measures Mediating Membrane Potentials Mitochondria Mitogen-Activated Protein Kinases Molecular Morphology Mus Neuronal Plasticity Neurons Oxygen Oxygen Consumption PECAM1 gene Pathologic Pathway interactions Patients Pattern Permeability Production Rattus Recombinants Recovery Recovery of Function Recycling Signal Pathway Signal Transduction Small Interfering RNA Stem cells Stroke System Testing Time Vascular remodeling Western Blotting angiogenesis brain endothelial cell brain remodeling central nervous system injury deprivation extracellular immunocytochemistry improved in vivo kinase inhibitor microscopic imaging mitochondrial membrane neural growth neurological recovery neurovascular neurovascular unit neutralizing antibody new therapeutic target novel optical imaging particle post stroke potential biomarker progenitor public health relevance relating to nervous system repaired spatiotemporal stroke recovery synaptogenesis

项目摘要

DESCRIPTION (provided by applicant): Reactive astrocytes were traditionally thought to induce both detrimental and beneficial effects for brain remodeling after stroke. Here, we propose a new concept whereby reactive astrocytes can surprisingly transfer mitochondria into adjacent neurons and endothelial cells to promote neurovascular remodeling in damaged brain. Our overall hypothesis is as follows. Damage associated molecular pattern (DAMP) signals upregulate CD38 in reactive astrocytes. In addition, accumulating endothelial progenitor cells (EPCs) secrete soluble CD31 that further amplify CD38 signaling. Altogether, this gliovascular crosstalk induces astrocytes to release of extracellular particles containing mitochondria. Mitochondria are then transferred into neurons and endothelium, thus enhancing neuroplasticity, BBB repair, angiogenesis and overall neurovascular recovery. Our pilot data are intriguing: (i) DAMPs or soluble CD31 upregulate CD38 in astrocytes, (ii) CD38 signaling causes astrocytes to release extracellular mitochondria, (iii) confocal microscopy reveals transfer of astrocytic mitochondria into neurons and endothelial cells, (iv) extracellular mitochondria enhance neural growth and angiogenesis, (v) suppression of astrocytic CD38 with siRNA inhibits neuronal plasticity after focal ischemia, and (vi) extracellular particles with functional mitochondria can e detected in CSF from human stroke patients. We will test 3 specific aims in this project. In Aim 1, we will investigate mechanisms of extracellular mitochondria particle production in reactive astrocytes. In Aim 2, we will dissect mechanisms of astrocytic mitochondria transfer for enhancing neurovascular remodeling. Finally in Aim 3, we will demonstrate that remodeling vascular signals promote mitochondria transfer from reactive astrocytes into neurons and endothelial cells after stroke in vivo. This study should define a novel mechanism of glial-EPCs crosstalk to enhance neurovascular remodeling and provide a new concept for mitochondrial transfer in the neurovascular unit.

描述（由申请人提供）：传统上认为反应性星形胶质细胞对中风后的脑重塑既有有害作用，也有有益作用。在这里，我们提出了一个新的概念，即反应性星形胶质细胞可以令人惊讶地将线粒体转移到邻近的神经元和内皮细胞，以促进受损脑中的神经血管重塑。我们的总体假设如下。损伤相关分子模式（DAMP）信号上调反应性星形胶质细胞中的CD38。此外，积聚的内皮祖细胞（EPC）分泌进一步放大CD38信号传导的可溶性CD31。总而言之，这种胶质血管串扰诱导星形胶质细胞释放含有线粒体的细胞外颗粒。然后将线粒体转移到神经元和内皮细胞中，从而增强神经可塑性、BBB修复、血管生成和整体神经血管恢复。我们的试点数据很有趣：（i）DAMP或可溶性CD 31上调星形胶质细胞中的CD 38，（ii）CD 38信号传导导致星形胶质细胞释放细胞外线粒体，（iii）共聚焦显微镜显示星形胶质细胞线粒体转移到神经元和内皮细胞中，（iv）细胞外线粒体增强神经生长和血管生成，（v）用siRNA抑制星形胶质细胞CD 38抑制局灶性缺血后的神经元可塑性，和（vi）在来自人中风患者的CSF中可以检测到具有功能性线粒体的细胞外颗粒。我们将在这个项目中测试3个具体目标。在目的1中，我们将研究反应性星形胶质细胞中细胞外线粒体颗粒产生的机制。在目标2中，我们将剖析星形胶质细胞线粒体转移增强神经血管重塑的机制。最后，在目标3中，我们将证明在体内中风后重塑血管信号促进线粒体从反应性星形胶质细胞转移到神经元和内皮细胞。本研究为阐明胶质细胞与内皮祖细胞相互作用促进神经血管重构提供了新的机制，并为神经血管单位中线粒体的转移提供了新的概念。